|
1171
|
|
|
Collagen type XXVII alpha 1 chain |
STLS |
|
|
1172
|
|
|
Carboxypeptidase Z |
- |
|
|
1173
|
|
|
Calcium/calmodulin dependent protein kinase I |
CAMKI |
|
|
1174
|
|
|
Cyclin B3 |
CYCB3 |
|
|
1175
|
|
|
Contactin associated protein family member 4 |
CASPR4 |
|
|
1176
|
|
|
Cell division cycle 14A |
DFNB105, DFNB32, DFNB35, cdc14, hCDC14 |
|
|
1177
|
|
|
Cyclin dependent kinase 10 |
ALSAS, PISSLRE |
Al kaissi syndrome, Clinodactyly, Congenital epicanthus, Developmental delay, Dwarfism, Melanoma, Mental retardation, Microcephaly, Nasopharyngeal carcinoma, Posteriorly rotated ear, Synophrys |
|
1178
|
|
|
Caveolin 1 |
BSCL3, CGL3, LCCNS, MSTP085, PPH3, VIP21 |
Acanthosis nigricans, Arthritis, Atherosclerosis, Atrial fibrillation, Breast cancer, Mammary neoplasms, Breast carcinoma, Cirrhosis, Congenital lipodystrophy, Congestive heart failure, Crest syndrome, Diabetes mellitus, Diffuse cutaneous systemic sclerosis, Dwarfism, Dysphagia, Fatty liver, Gastric cancer, Gastroesophageal reflux disease, Glaucoma, Heritable pulmonary arterial hypertension, Hypercholesterolemia, Hyperinsulinism, Hypertension, Hypertrophic cardiomyopathy, Immunologic deficiency syndromes, Isolated somatotropin deficiency, Kidney disease, Limited systemic sclerosis, Lipoatrophic diabetes mellitus, Lipoatrophy, Lipodystrophy, Liver failure, Lung neoplasms, Lung cancer, Malabsorption syndrome, Malocclusion, Marfan syndrome, Mental retardation, Myocardial infarction, Myopathy, Nervous system diseases, Nystagmus, Osteopenia, Osteoporosis, Ovarian neoplasm, Ovarian cancer, Pancreatitis, Paroxysmal atrial fibrillation, Partial lipodystrophy, Partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome, Physiologic amenorrhea, Polycystic ovary syndrome, Precocious puberty, Prostatic neoplasms, Prostate cancer, Pulmonary arterial hypertension, Pulmonary fibrosis, Pulmonary hypertension, Pulmonary hypertension with hereditary hemorrhagic telangiectasia, Renal glomerular disease, Renal insufficiency, Retinitis pigmentosa, Schizophrenia, Scleroderma, Scoliosis, Open angle glaucoma, Secondary physiologic amenorrhea, Somatotropin deficiency, Stevens-johnson syndrome, Stomach neoplasms, Talipes transversoplanus, Ventricular hypertrophyView all (57 more) |
|
1179
|
|
|
Calcium/calmodulin dependent serine protein kinase |
CAGH39, CAMGUK, CMG, FGS4, LIN2, MICPCH, MRXSNA, TNRC8, hCASK |
Anaplastic carcinoma, Anemia, Autism, Carcinoma, Cataract, Cerebellar atrophy, Cerebellar diseases, Cerebellar hypoplasia, Cerebral cortical atrophy, Choreoathetosis, Clonic seizures, Congenital epicanthus, Congenital exomphalos, Congenital microcephaly, Developmental delay, Developmental regression, Dwarfism, Dyskinetic syndrome, Dysmorphic features, Dyssomnia, Epileptic encephalopathy, Episodic ataxia, Febrile seizures, Fg syndrome, Fg syndrome phenotypic spectrum, Focal seizures, Fundus coloboma, Hearing loss, High palate, Hyperbilirubinemia, Hypohidrosis, Hypoplasia of corpus callosum, Hypoplasia of the optic nerve, Hypotonic seizures, Lung carcinoma, Macrotia, Mental retardation, Mental retardation and microcephaly with pontine and cerebellar hypoplasia, Mental retardation, x-linked, Microcephaly, Micrognathism, Microlissencephaly, Movement disorders, Multiple congenital anomalies, Myopia, Hypotonia, Neurodevelopmental disorders, Nystagmus, Optic atrophy, Pachygyria, Partington syndrome, Penis agenesis, Pontoneocerebellar hypoplasia, Precocious puberty, Renal dysplasia, Retinal coloboma, Scoliosis, Seizure, Sleep disorders, Strabismus, Ureterocele, Ventricular septal defect, West syndromeView all (48 more) |
|
1180
|
|
|
Caveolin 2 |
CAV |
|
